rs202047589

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs202047589(C;T)

Make rs202047589(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

97599780

Gene

HOGA1

is a	snp
is	mentioned by
dbSNP	rs202047589
dbSNP (classic)	rs202047589
ClinGen	rs202047589
ebi	rs202047589
HLI	rs202047589
Exac	rs202047589
Gnomad	rs202047589
Varsome	rs202047589
LitVar	rs202047589
Map	rs202047589
PheGenI	rs202047589
Biobank	rs202047589
1000 genomes	rs202047589
hgdp	rs202047589
ensembl	rs202047589
geneview	rs202047589
scholar	rs202047589
google	rs202047589
pharmgkb	rs202047589
gwascentral	rs202047589
openSNP	rs202047589
23andMe	rs202047589
SNPshot	rs202047589
SNPdbe	rs202047589
MSV3d	rs202047589
GWAS Ctlg	rs202047589

Max Magnitude

0

ClinVar
Risk	rs202047589(T;T)
Alt	rs202047589(T;T)
Reference	Rs202047589(C;C)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	HOGA1
CLNDBN	Primary hyperoxaluria, type III
Reversed	0
HGVS	NC_000010.10:g.99359537C>T
CLNSRC
CLNACC	RCV000186480.1,